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piRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective
Mutations in the MECP2 gene are found in a large proportion of girls with Rett Syndrome. Despite extensive research, the principal role of MeCP2 protein remains elusive. Is MeCP2 a regulator of genes, acting in concert with co-activators and co-repressors, predominantly as an activator of target gen...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
IOS Press
2012
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3810717/ https://ncbi.nlm.nih.gov/pubmed/22976001 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2012-0932 |
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